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Abstract

Grant Number: 1R43HL087456-01
Project Title: Apyrase to Treat Ischemia/Reperfusion Injury during Lung Transplantation
PI Information:NameEmailTitle
CHEN, RIDONG rchen@niduscenter.com

Abstract: DESCRIPTION (provided by applicant): Human apyrase represents a highly promising therapy to reduce ischemia/reperfusion injury which occurs in10-20% of lung transplant recipients as the consequence of unavoidable processes of procurement, preservation and restoring blood flow. This clinical condition, recently termed primary graft dysfunction, remains an important problem after lung transplantation, and still represents the single biggest cause of early morbidity and mortality for lung recipients. Apyrase strongly inhibits platelet activation and inflammation with modest bleeding risk. Using a protein informatics approach, we have successfully engineered a clot-targeting human apyrase, APT202, which exhibits significantly higher enzymatic activity and platelet inhibition than the wild-type apyrase. With the Phase I SBIR grant support, we will optimize the dose regimen of APT202 that will provide significant benefits while maintaining low bleeding risk in established animal transplantation models. The ultimate goal is to advance APT202 into clinic to improve patient outcome in terms of oxygenation improvement, reduction for duration of mechanical ventilation and hospital stay. Human apyrase represents a highly promising therapy to reduce ischemia/reperfusion injury associated with lung transplantation. We will optimize the dose regimen of a clot- targeting apyrase that will provide significant benefits while maintaining low bleeding risk in established animal transplantation models.

Thesaurus Terms:
cardiovascular disorder chemotherapy, drug screening /evaluation, enzyme activity, ischemia, lung transplantation, medical complication, nonhuman therapy evaluation, reperfusion
CHO cell, antiinflammatory agent, cardiovascular disorder prevention, chemoprevention, drug administration rate /duration, gene expression, inhibitor /antagonist, membrane protein, platelet activation
intravenous administration, laboratory rat, molecular cloning

Institution: APT THERAPEUTICS, INC.
893 NORTH WARSON ROAD
SAINT LOUIS, MO 63141
Fiscal Year: 2007
Department:
Project Start: 01-MAY-2007
Project End: 30-APR-2008
ICD: NATIONAL HEART, LUNG, AND BLOOD INSTITUTE
IRG: ZRG1


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